Seminars in Oncology
Volume 30, Issue 5 , Pages 649-658, October 2003

Immunotherapy for prostate cancer

  • Lawrence Fong

      Affiliations

    • Departments of Medicine, and Microbiology/Immunology, University of California, San Francisco, San Francisco, CA, USA
    • Corresponding Author InformationAddress reprint requests to Lawrence Fong, MD, UCSF Comprehensive Cancer Center, 1600 Divisadero St, Box 1711, San Francisco, CA 94143-1711, USA
  • ,
  • Eric J Small

      Affiliations

    • Departments of Medicine and Urology, University of California, San Francisco, San Francisco, CA, USA

Abstract 

While androgen deprivation has remained the cornerstone of therapy for advanced prostate cancer over the last 60 years, novel therapies are being developed that may expand upon currently available treatments. The identification of antigens expressed by prostate tissue and/or prostate cancer that are recognized by T cells creates opportunities to develop novel immunotherapeutic approaches, including tumor vaccines. Improved understanding of immune recognition and antigen presentation may lead to effective immunotherapies for prostate cancer. Identified proteins expressed in prostate cancer, including prostate-specific antigen (PSA), prostatic acid phosphatase (PAP), and prostate-specific membrane antigen (PSMA), have been used as immunologic targets for immunotherapy. Moreover, innovations in cancer genomics and proteomics will also aid in the identification of immunologic targets. Immunotherapy trials have already demonstrated evidence of not only immunogenicity, but also clinical efficacy, and future studies will be directed at capitalizing on these findings.

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 Supported by by CapCure and NIH NCI Grant No. K23 CA82584-01.

PII: S0093-7754(03)00350-6

doi:10.1016/S0093-7754(03)00350-6

Seminars in Oncology
Volume 30, Issue 5 , Pages 649-658, October 2003